Research at Hughes Spalding. Updated Review and Approval Process
Navigate the research review and approval process efficiently as a busy clinician investigator at Hughes Spalding with insights on key responsibilities, approval levels, and contact information of relevant personnel. From pre-award tasks like facilitating reviews and gaining approvals to post-award
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Title IX Training
Title IX regulations mandate that educational institutions provide training to personnel involved in addressing sexual harassment and discrimination. This training covers defining sexual harassment, conducting investigations impartially, avoiding bias, and ensuring fair treatment in grievance proces
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HER2 Tyrosine Kinase Inhibitor Zongertinib Phase Ia/b Trial in Solid Tumors
Study on Zongertinib, a HER2 tyrosine kinase inhibitor, in patients with HER2 aberration-positive solid tumors. The trial involves multiple centers worldwide and aims to evaluate the efficacy of Zongertinib in treating various cancers harboring HER2 mutations. Financial disclosures of lead investiga
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Huntington's Disease Research Opportunities with Dr. Jamie Herron
Dr. Jamie Herron, a Consultant Psychiatrist specializing in Huntington's Disease, presents research opportunities including sub-investigator roles in clinical trials like Wave SNP3 and biomarker studies. The portfolio outlines the genetic basis of Huntington's, associated symptoms, and the chance to
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Transitioning to Leadership Roles in Research: Challenges and Responsibilities
Explore the journey of transitioning into leadership roles in research, uncovering different leadership styles, tips for success, and the responsibilities and challenges that come with becoming a Principal Investigator. Learn how to navigate the transition, inspire your team, and effectively manage
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Embracing Team Science in Research: A Comprehensive Guide
Explore the transition from investigator-driven to large-team research, understanding the essence of team science, its benefits, challenges, and the stages of team development. Learn the critical aspects of forming, storming, and norming teams before writing a grant, emphasizing shared vision, confl
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Cybersecurity Expert Shiva V. Parasram - Profile and Advice
Shiva V. Parasram is a renowned figure in cybersecurity, serving as a Director, Cybersecurity Instructor, Penetration Tester, and Forensic Investigator. He shares valuable insights, tools, and tips for handling security breaches and hacks effectively, along with essential advice for safeguarding you
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Provider Training Programs for Event Management Alignment
This collection of training programs focuses on event management alignment for executive, management staff, and direct care professionals in the service provider industry. The programs cover responsibilities, protocols, and processes related to reportable event management in various service provider
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Villanova IRB New Investigator Training Overview
Human Subject Research Protections at Villanova IRB, including regulatory background, review process, and key information for investigators. Learn about the Institutional Review Board structure, ethical principles, and historical background of human subjects research at Villanova University.
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Understanding Regulatory Requirements of Drugs and Pharmaceuticals
Drug regulation involves controlling drug use through international agreement authorities like the FDA, EMA, and PMDA. The FDA plays a crucial role in drug evaluation and research, biologic evaluation, devices, and food safety. There are various types of applications for drug approval, along with a
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Understanding IRB Reliance Agreements in Research
IRB reliance agreements allow institutions to delegate IRB review responsibilities or collaborate with other institutions for human subjects research. Federalwide assurance (FWA) documents ensure compliance with regulations. Different types of agreements, such as IRB authorization agreements and ind
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POSNOC & ATNEC Trials Update by Amit Goyal: Investigating Axillary Treatment in Breast Cancer
POSNOC (Positive Sentinel Node) and ATNEC trials are investigating the effectiveness of axillary treatment in women with early-stage breast cancer having metastases in one or two sentinel nodes. Led by Chief Investigator Amit Goyal in the UK, this randomized controlled trial compares adjuvant therap
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Understanding the Notice of Award in Research Grants Management
The Notice of Award (NoA) is a crucial document in the grants management process that legally binds the grantee and establishes funding levels and conditions. It includes key information such as the grantee's details, principal investigator, funding period, and contact information. The NoA has stand
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Transition to Leading a Research Team: A Guide for Emerging Leaders
Explore the journey of transitioning into a leadership role within a research team, covering different leadership styles, challenges, responsibilities, and tips for success. Gain insights on what to expect as you progress to becoming a Principal Investigator, managing funding, research advancement,
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Comparison of FFR-guided PCI vs Angiography-guided PCI in AMI with Multivessel Disease: FRAME-AMI Trial
In patients with acute myocardial infarction (AMI) and multivessel coronary artery disease, this study aims to compare fractional flow reserve (FFR)-guided PCI with angiography-guided PCI for non-infarct-related artery lesions. The hypothesis is that selective PCI guided by FFR is superior to routin
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Ensuring Protocol Compliance and Corrective Action Plans in Clinical Trials
This content discusses the importance of creating Corrective Action and Preventive Action (CAPA) plans for protocol deviations in clinical trials. It covers the components of a CAPA, best practices for creating CAPAs for different deviation types, and regulatory compliance requirements according to
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REDCap Cloud: Advancing Clinical Trials with Enhanced Features
Streamline your clinical trial processes with REDCap Cloud, a secure and validated platform offering improved user interface, pre-configured ePRO, and compliance with regulations. Benefit from free licensing for investigator-initiated trials and explore the easy setup steps for creating forms and ev
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Investigator Roles and Responsibilities in Clinical Research
Key responsibilities of investigators in clinical research involve ensuring participant safety, compliance with regulations, accurate data collection, and ethical conduct throughout the study process. Properly trained investigators play a crucial role in the success and integrity of clinical trials.
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Principal Investigator Responsibilities in Clinical Trials
The Principal Investigator (PI) plays a crucial role in conducting clinical trials. Responsibilities include overseeing the trial at the site, making critical decisions, ensuring compliance with protocols, obtaining informed consent, maintaining accurate records, and more. Non-compliance can lead to
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Data Editing and Coding Processes in Research
Data editing involves the detection and correction of errors in raw data to ensure accuracy and consistency. It includes field editing, where investigator reviews data for completeness, and central editing for thorough editing on completed forms. The coding process assigns symbols to responses for a
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Best Practices for Subrecipient Monitoring in Research Projects
Effective management of subawards in research projects requires collaboration, clear responsibilities, financial monitoring, and technical oversight. This involves building strong relationships with stakeholders, including the Principal Investigator and subawardee, and ensuring compliance with spons
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Embedded Research Conference Workgroup B: Management Decisions Support
Workgroup B at the Embedded Research Conference focuses on providing research support for management decisions. The participants aim to identify and prioritize operational questions that could benefit from embedded research, work productively within the existing QI ecosystem, and create an inventory
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Study on Juvenile Drug Crime Prevention in Taiwan: Insights from ACS Conference 2020
This presentation at the Asian Criminological Society Conference 2020 delves into the current situation, dilemmas, and responses regarding juvenile drug crime prevention in Taiwan. The presenter, Zeng Li-Wen, a PhD student at Central Police University in Taiwan, provides valuable insights based on t
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Rural Access Compliance Rules Proposal by Glenn Disher - PBM Investigator
Proposal by Glenn Disher, a PBM Compliance Investigator, outlines rules for rural access compliance. The proposal focuses on considering local conditions and enforcing rules for maximum impact. It includes recommendations for zip code rules, compliance mileage rules, and examples of non-compliant ru
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Guide to Material Transfer Agreements and Data Negotiations in Research
Explore the key aspects of Material Transfer Agreements (MTAs), Confidentiality Agreements, and Data Use Agreements in research projects. Learn about the types of agreements negotiated, entities involved, the process for obtaining fully executed agreements, and how to get started as a Principal Inve
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Research Ethics in Child Psychiatry: Introduction and Historical Perspectives
This presentation provides an introduction to research ethics in child psychiatry, emphasizing the importance of ethical considerations in conducting studies involving children. It highlights key ethical principles, historical events shaping research ethics, and examples of past unethical practices.
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GMAS Proposal Entry and Homepage Enhancements Overview
GMAS Proposal Entry and Proposal Homepage are undergoing enhancements, consolidating multiple screens into one for Initial Proposal and Competing Renewal entries. Changes include smarter organization look-up, streamlined principal investigator search, new sponsor look-up, and automatic period genera
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Sponsor Expectations for Clinical Studies at Thomas Jefferson University
This presentation discusses the sponsor expectations for clinical studies, investigator responsibilities, TJU's strengths in conducting studies, and how principal investigators can impress sponsors. Topics include assessment of investigator performance, regulatory guidelines, streamlining processes,
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Initiating Sponsored Projects: A Comprehensive Guide
Explore the process of starting sponsored projects including the role of the Principal Investigator, required forms for personnel, proposal development steps, and review considerations before submission. Understand key aspects such as financial conflict of interest policies, intellectual property ag
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Hire the Best Private Investigator in Malibu at Kinsey Investigations
As the leading private investigator in Malibu, Kinsey Investigations offers a wide array of services tailored to your needs. Our experienced team is adept at handling sensitive cases, ensuring confidentiality and professionalism at every step. From p
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Hire the Best Private Investigator in Malibu
As the leading private investigator in Malibu, Kinsey Investigations offers a wide array of services tailored to your needs. Our experienced team is adept at handling sensitive cases, ensuring confidentiality and professionalism at every step. From p
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Choose The Best Private Investigator in Malibu
As the leading private investigator in Malibu, Kinsey Investigations offers a wide array of services tailored to your needs. Our experienced team is adept at handling sensitive cases, ensuring confidentiality and professionalism at every step. From p
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Guidelines for Academic Promotions in Medical School
Academic promotions in a medical school are crucial for recognizing achievements, maintaining competitiveness, and serving the institution's interests. Promotion criteria include teaching effectiveness, scholarly activity, clinical service, and active participation in various communities. Meritoriou
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Private Investigator in Malibu
Seeking a reliable Private Investigator in Malibu? Kinsey Investigations specializes in discreet and effective solutions for all your investigative needs. Contact us today for professional assistance you can trust.
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Understanding Pharmacology and Toxicology in Investigator Brochures
Explore the essential aspects of pharmacology and toxicology covered in Investigator Brochures, including nonclinical information, safety pharmacology, general toxicology, genetic toxicology, and more. Learn about the significance of pharmacology in predicting intended and unintended effects, consid
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Understanding Discrimination Investigations in Business Settings
Explore the role of a Civil Rights Investigator like Rob Rowan Sr. from the Lincoln Commission on Human Rights in conducting discrimination investigations in housing, employment, and public accommodations. Learn about the investigation process, burden shifting, and the impact on businesses in terms
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Best Practices for Conducting a Fair Investigation
Explore the key elements of conducting an effective investigation, including determining scope, developing a plan, and remaining impartial. Learn about common investigation mistakes to avoid and the importance of thoroughness in reporting. Understand the role of the investigator and considerations f
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Title IX Complaint Process Investigator Training Overview
This content provides a comprehensive guide to Title IX, including its purpose, procedures, training requirements, and the role of investigators and advisors in the complaint process. It covers the definition of Title IX, the purpose of procedures, the hearing process, and the training requirements
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Insights into Information Terrorism from IT Forensics Perspective
Delve into the world of terrorism and information technology through the lens of IT forensics. Explore topics such as the uncertainties surrounding cybersecurity and digital crimes, the role of security players, Locard's Exchange Principle, computer investigations, evidence analysis, investigator qu
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Challenges and Concerns in Immunology Research Funding: Investigator's Perspective
Investigator's face challenges in understanding NIH funding priorities, decreases in basic science grants, disease-earmarked funding changes, application logistics confusion, grant funding mechanisms variations, new rigorous research requirements, and equity in grant budgets.
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